HNRNPA3 Antibody

1. This study showed that HNRNPA3 variants identified in Australian patients with familial amyotrophic lateral sclerosis (FALS) and associated alternate allele frequencies in cases and controls. PMID: 29131108
2. Study investigated the pattern of hnRNP A1, A2/B1 and A3 immunostaining across a range of clinical, pathological and genetic forms of Frontotemporal Lobar Degeneration and Motor Neurone Disease. Data suggest there might be a derangement of movement of hnRNP A1, and other hnRNP proteins, across all pathological forms of Frontotemporal Lobar Degeneration beyond that involving just TDP-43 or FUS. PMID: 28431575
3. Neurons in the hippocampus of C9orf72 patients are frequently devoid of hnRNPA3. Reduced nuclear hnRNPA3 in the hippocampus of patients with extended C9orf72 repeats correlates with increased DPR deposition. PMID: 27461252
4. The results of this study suggested that mutations in hnRNPA1, A2/B1, and A3 genes are a rare finding in amyotrophic lateral sclerosis. PMID: 23827524
5. characterization of hnRNP A3 in human and mouse cell lines PMID: 22546510
6. Results suggest that hnRNP A3 is associated with telomere in vivo and acts as a negative regulator of telomere length maintenance. PMID: 20600361
7. These biochemical properties of hnRNP A3 suggest that hnRNP A3 can participate in telomere regulation in vivo. PMID: 17919748

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HGNC: 24941

OMIM: 605372

KEGG: hsa:220988

STRING: 9606.ENSP00000376309

UniGene: Hs.516539